KR900004681A - 이중 차단된 트리이소시아네이트 화합물의 제조방법 - Google Patents

이중 차단된 트리이소시아네이트 화합물의 제조방법 Download PDF

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KR900004681A
KR900004681A KR1019890013876A KR890013876A KR900004681A KR 900004681 A KR900004681 A KR 900004681A KR 1019890013876 A KR1019890013876 A KR 1019890013876A KR 890013876 A KR890013876 A KR 890013876A KR 900004681 A KR900004681 A KR 900004681A
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South Korea
Prior art keywords
blocked
diisocyanate
double
nco
different
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KR1019890013876A
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English (en)
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KR930004359B1 (ko
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파르 빌리발드
그모서 요한
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헬무트 스트라메츠, 한스-디이터 하누스
비아노바 쿤스트 하르쯔 아크티엔게젤샤프트
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C269/00Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C269/02Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups from isocyanates with formation of carbamate groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/46Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
    • C07C275/58Y being a hetero atom
    • C07C275/60Y being an oxygen atom, e.g. allophanic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78Nitrogen
    • C08G18/7806Nitrogen containing -N-C=0 groups
    • C08G18/7818Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78Nitrogen
    • C08G18/7806Nitrogen containing -N-C=0 groups
    • C08G18/7818Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
    • C08G18/7837Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing allophanate groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/80Masked polyisocyanates
    • C08G18/8061Masked polyisocyanates masked with compounds having only one group containing active hydrogen

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Paints Or Removers (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

내용 없음

Description

이중 차단된 트리이소시아네이트 화합물의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (6)

  1. 완전 차단된 디이소시아네이트 1몰을 촉매의 존재 또는 부재하에 70 내지 120℃에서(여기서 최고 반응 온도는 유리 NCO 그룹의 반응 및/또는 차단제의 분해가 일어나지 않는 온도를 선택한다) NCO 그룹의 반응성이 현저히 상이한 비-차단된 디이소시아네이트 1몰과, 모노이소시아네이트 화합물에 상응하는 NCO값에 도달될 때까지 반응시킴을 특징으로 하여, 이중차단된 트리이소시아네이트 화합물을 제조하는 방법.
  2. 제1항에 있어서, 비-차단된 디이소시아네이트의 첨가를 70℃에서 출발하여 온도를 상승시키면서 수행함을 특징으로 하는 방법.
  3. 제1항 또는 2항에 있어서, 2,6-이성체를 20중량% 이하로 함유하는 공업용 2,4-톨루일렌 디이소시아네이트를 비-차단된 디이소시아네이트로 사용함을 특징으로 하는 방법.
  4. 다음 일반식의 이중 차단된 트리이소시아네이트.
    상기식에서, R은 디이소시아네이트로부터 유도되는 지방족, 지환족 또는 방향족 라디칼이고, R1은 NCO 그룹의 반응성이 현저히 상이한 디이소시아네이트로부터 유도되는 지방족, 지환족 또는 방향족 라디칼이며, R2및 R3는 NCO 차단제의 동일하거나 상이한 라디칼이다.
  5. 제4항에 있어서, 라디칼 R이 상이한 반응성의 NCO 그룹을 갖는 디이소시아네이트로부터 유도된 것임을 특징으로 하는 이중차단된 트리이소시아네이트.
  6. 하이드록실 그룹 및/또는 1급 및/또는 2급 아미노 그룹을 포함하는 페인트 결합제용 가교결합 성분으로서, 바람직하게는 상기와 같은 페인트 결합제에 차단된 우레탄 가교결합 그룹을 도입시키기 위한, 제4항 내지 5항중 어느 한 항에 따르는 이중차단된 트리이소시아네이트의 용도.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890013876A 1988-09-29 1989-09-27 이중 차단된 트리이소시아네이트 화합물의 제조방법 KR930004359B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AT0240188A AT390788B (de) 1988-09-29 1988-09-29 Neue diblockierte triisocyanatverbindungen, ein verfahren zu ihrer herstellung und ihre verwendung
ATA2401/88 1988-09-29

Publications (2)

Publication Number Publication Date
KR900004681A true KR900004681A (ko) 1990-04-12
KR930004359B1 KR930004359B1 (ko) 1993-05-26

Family

ID=3533679

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Application Number Title Priority Date Filing Date
KR1019890013876A KR930004359B1 (ko) 1988-09-29 1989-09-27 이중 차단된 트리이소시아네이트 화합물의 제조방법

Country Status (6)

Country Link
EP (1) EP0362654B1 (ko)
JP (1) JPH02134356A (ko)
KR (1) KR930004359B1 (ko)
AT (1) AT390788B (ko)
DE (1) DE58902690D1 (ko)
ES (1) ES2045327T3 (ko)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4441176A1 (de) * 1994-11-18 1996-05-23 Bayer Ag Allophanatgruppen aufweisende Polyisocyanate
US6214470B1 (en) 1998-12-21 2001-04-10 Basf Corporation Cathodic electrocoat composition
US6228472B1 (en) * 1998-12-21 2001-05-08 Basf Corporation Process for synthesis of allophanate compounds and compositions including the product thereof
WO2019051341A2 (en) * 2017-09-08 2019-03-14 Maple Ridge, Llc OIL COPOLYMERS FOR TISSUE FASTENERS

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2729990A1 (de) * 1977-07-02 1979-01-18 Bayer Ag Verfahren zur herstellung von isocyanatgruppen aufweisenden allophanaten
US4423171A (en) * 1981-12-28 1983-12-27 Ford Motor Company Tertiary alcohol-diblocked diisocyanate diurea oligomers and coating compositions comprising same
AT383604B (de) * 1985-11-05 1987-07-27 Vianova Kunstharz Ag Verfahren zur herstellung von mono- oder polyisocyanatverbindungen und deren verwendung

Also Published As

Publication number Publication date
JPH02134356A (ja) 1990-05-23
KR930004359B1 (ko) 1993-05-26
DE58902690D1 (de) 1992-12-17
EP0362654B1 (de) 1992-11-11
ATA240188A (de) 1989-12-15
AT390788B (de) 1990-06-25
ES2045327T3 (es) 1994-01-16
EP0362654A1 (de) 1990-04-11

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